SCOPUS 정보 검색 플랫폼

Volumn 103, Issue 4, 2001, Pages 283-288

Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES Syndrome): A newly recognized autosomal recessive syndrome

(3) Kantaputra, Piranit N a Kunachaichote, Jurairat a Patikulsila, Prapatsorn b

a CHIANG MAI UNIVERSITY (Thailand)

b Faculty of Medicine Chiang Mai University (Thailand)

Author keywords

Atopic dermatitis blepharophimosis blepharoptosis cone shaped epiphysis hyperopic astigmatism; Mandibular prognathism; Mental retardation; Obesity

Indexed keywords

ABDUCENS NERVE PARALYSIS; ARTICLE; ASTIGMATISM; ATOPIC DERMATITIS; AUTOSOMAL RECESSIVE DISORDER; BLEPHAROPHIMOSIS; CASE REPORT; CONVERGENT STRABISMUS; CRANIOFACIAL MALFORMATION; EYE MALFORMATION; FEMALE; HUMAN; MACROCEPHALY; MAXILLA HYPOPLASIA; MENTAL DEFICIENCY; MOMES SYNDROME; OBESITY; PRIORITY JOURNAL; PROGNATHIA; PTOSIS; SCHOOL CHILD; SKIN DISEASE; SPEECH DISORDER; THAILAND; TOE MALFORMATION; TOOTH MALFORMATION; VISUAL ACUITY;

ABNORMALITIES, MULTIPLE; CHILD; DIAGNOSIS, DIFFERENTIAL; EYE ABNORMALITIES; FEMALE; GENES, RECESSIVE; HUMANS; MENTAL RETARDATION; OBESITY; PROGNATHISM; SKIN ABNORMALITIES; SYNDROME;

EID: 0035500257 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.1572 Document Type: Article

Times cited : (10)

References (11)

1
- 0031040854
- Bardet-Biedl syndrome: A molecular and phenotypic study of 18 families
- (1997) J Med Genet , vol.34 , pp. 92-98
- Beales, P.L.¹ Warner, A.M.² Hitman, G.A.³ Thankker, R.⁴ Flinter, F.A.⁵

2
- 0031984609
- Blepharophimosis: A causally heterogeneous malformation frequently associated with developmental disabilities
- (1998) Am J Med Genet , vol.75 , pp. 52-54
- Cunniff, C.¹ Curtis, M.² Hassed, S.J.³ Hoyme, H.E.⁴

3
- 0034665201
- Identification of BPESC1, a novel gene disrupted by a balanced chromosomal translocation, t(3;4)(q23;p15.2), in a patient with BPES
- (2000) Genomic , vol.68 , pp. 296-304
- De Baere, E.¹ Fukushima, Y.² Small, K.³ Udar, N.⁴ Camp, G.V.⁵ Verhoeven, K.⁶ Palotie, A.⁷ De Paepe, A.⁸ Messiaen, L.⁹

4
- 0023852163
- Bardet-Biedl and Laurence-Moon syndromes in a mixed Arab population
- (1988) Clin Genet , vol.33 , pp. 78-82
- Farag, T.I.¹ Teebi, A.S.²

5
- 0034608284
- Homozygosity mapping in a family with microcephaly, mental retardation, and short stature to a Cohen syndrome region on 8q21.3-8q22.1: Redefining a clinical entity
- (2000) Am J Med Genet , vol.92 , pp. 285-292
- Horn, D.¹ Krebsova, A.² Kunze, J.³ Reis, A.⁴

6
- 0033756314
- Ophthalmologic findings in Cohen syndrome. A long-term follow-up
- (2000) Ophthalmology , vol.107 , pp. 1737-1745
- Kivitie-Kallio, S.¹ Summanen, P.² Raitta, C.³ Norio, R.⁴

7
- 0032866339
- The Camera-Marugo-Cohen syndrome: Report of two new patients
- (1999) Am J Med Genet , vol.86 , pp. 208-214
- Lambert, D.M.¹ Watters, G.² Andermann, F.³ Der Kaloustian, V.M.⁴

8
- 0032079335
- Vertical transmission of the Ohdo blepharophimosis syndrome
- (1998) Am J Med Genet , vol.77 , pp. 144-148
- Mhanni, A.A.¹ Dawson, A.J.² Chudley, A.E.³

9
- 0027319724
- Macrosomia, obesity, macrocephaly and ocular abnormalities (MOMO syndrome) in two unrelated patients: Delineation of newly recognized overgrowth syndrome
- (1993) Am J Med Genet , vol.46 , pp. 555-558
- Moretti-Ferreira, D.¹ Koiffmann, C.P.² Listik, M.³ Setian, N.⁴ Wajntal, A.⁵

10
- 0034640677
- Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with mosaic trisomy 15
- (2000) Am J Med Genet , vol.93 , pp. 215-218
- Olander, E.¹ Stamberg, J.² Steinberg, L.³ Wulfsberg, E.A.⁴

11
- 0033803114
- MOMO syndrome: A possible third case
- (2000) Clin Dysmorphol , vol.9 , pp. 281-284
- Zannolli, R.¹ Mostardini, R.² Hadjistilianou, T.³ Rosi, A.⁴ Berardi, R.⁵ Morgese, G.⁶

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.